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首页> 外文期刊>In vivo. >Erythropoietin receptors in endometrial carcinoma as related to HIF1{alpha} and VEGF expression.
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Erythropoietin receptors in endometrial carcinoma as related to HIF1{alpha} and VEGF expression.

机译:子宫内膜癌中的促红细胞生成素受体与HIF1α和VEGF表达有关。

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Erythropoietin receptors (EpoRs) are expressed in a large percentage of cells in many human malignancies, including endometrial adenocarcinoma. In such tumors, administration of recombinant human erythropoietin (rhEpo) during radiotherapy and chemotherapy may oppose tumor progression by interfering with growth and invasion pathways. In the present study, a strong EpoR expression was demonstrated in 58.8% of 72 stage I endometrial adenocarcinomas, and this pattern was linked with a high degree of tumor differentiation (p=0.01), deep myometrial invasion (p=0.04) and, marginally, with poor prognosis (p=0.06). In addition, a strong association with the immunohistochemical expression of hypoxia-inducible factor 1alpha (HIF1alpha) and the downstream angiogenic protein vascular endothelial growth factor (VEGF) was noted. In multivariate analysis, HIF1alpha, but not EpoR, was associated with the depth of myometrial invasion (p=0.04) and marginally with prognosis (p=0.07). It is concluded that EpoR are common constituents of endometrial adenocarcinomas and are related to tumor aggressiveness, although this is probably a result of their involvement in an active HIF pathway.
机译:促红细胞生成素受体(EpoRs)在许多人类恶性肿瘤(包括子宫内膜腺癌)的大量细胞中表达。在此类肿瘤中,在放疗和化疗过程中给予重组人促红细胞生成素(rhEpo)可能会干扰生长和侵袭途径,从而阻止肿瘤进展。在本研究中,在72个I期子宫内膜腺癌中有58.8%证实了EpoR的强表达,并且这种模式与高度的肿瘤分化程度(p = 0.01),深层子宫肌层浸润(p = 0.04)和边缘性息息相关。 ,预后较差(p = 0.06)。此外,还注意到与缺氧诱导因子1alpha(HIF1alpha)和下游血管生成蛋白血管内皮生长因子(VEGF)的免疫组织化学表达密切相关。在多变量分析中,HIF1alpha与肌层浸润深度(p = 0.04)相关,而与EpoR无关,而与预后相关(p = 0.07)。结论是,EpoR是子宫内膜腺癌的常见成分,并且与肿瘤侵袭性有关,尽管这可能是由于它们参与了活跃的HIF途径所致。

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